4.5 Article

Neuroimaging biomarkers and cognitive function in non-CNS cancer and its treatment: Current status and recommendations for future research

Journal

BRAIN IMAGING AND BEHAVIOR
Volume 7, Issue 4, Pages 363-373

Publisher

SPRINGER
DOI: 10.1007/s11682-013-9283-7

Keywords

Neuroimaging; MRI; PET; Cognition; Cancer; Chemotherapy; Genetics; Biomarkers; Personalized medicine

Categories

Funding

  1. National Cancer Institute [R01 CA101318, P30 CA082709, R25 CA117865]
  2. National Institute on Aging [R01 AG19771, P30 AG10133]
  3. National Library of Medicine [R01 LM011360]
  4. Dutch Cancer Society [KWF 2009-4284, KWF 2010-4894, KWF 2012 5495]
  5. Fonds Wetenschappelijk Onderzoek-Vlaanderen [G.048010N]
  6. Stichting tegen Kanker
  7. National Institute of Neurological Diseases and Stroke [R21 NS071385]

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Cognitive changes in patients undergoing treatment for non-central nervous system (CNS) cancers have been recognized for several decades, yet the underlying mechanisms are not well understood. Structural, functional and molecular neuroimaging has the potential to help clarify the neural bases of these cognitive abnormalities. Structural magnetic resonance imaging (MRI), functional MRI (fMRI), diffusion tensor imaging (DTI), MR spectroscopy (MRS), and positron emission tomography (PET) have all been employed in the study of cognitive effects of cancer treatment, with most studies focusing on breast cancer and changes thought to be induced by chemotherapy. Articles in this special issue of Brain Imaging and Behavior are devoted to neuroimaging studies of cognitive changes in patients with non-CNS cancer and include comprehensive critical reviews and novel research findings. The broad conclusions that can be drawn from past studies and the present body of new research is that there are structural and functional changes associated with cancer and various treatments, particularly systemic cytotoxic chemotherapy, although some cognitive and fMRI studies have identified changes at pre-treatment baseline. Recommendations to accelerate progress include well-powered multicenter neuroimaging studies, a better standardized definition of the cognitive phenotype and extension to other cancers. A systems biology framework incorporating multimodality neuroimaging, genetics and other biomarkers will be highly informative regarding individual differences in risk and protective factors and disease- and treatment-related mechanisms. Studies of interventions targeting cognitive changes are also needed. These next steps are expected to identify novel protective strategies and facilitate a more personalized medicine for cancer patients.

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